Core Viewpoint - The company reported its 1H25 performance, showing a slight decline in revenue but a significant increase in net profit, aligning with market expectations [1][2]. Financial Performance - Revenue for 1H25 was 4.356 billion yuan, a year-on-year decrease of 0.8% [1] - Net profit attributable to shareholders was 1.358 billion yuan, a year-on-year increase of 24.6% [1] - Adjusted net profit was 1.136 billion yuan, a year-on-year increase of 2.1%, meeting market expectations [1] Business Trends - Sales of core commercial products faced pressure in 1H25: - Revenue from Teva Australia was 2.371 billion yuan, down 4.2%, accounting for 54.4% of total revenue [1] - Revenue from Yibiao was 346 million yuan, down 12.1% [1] - Revenue from Cyber was 110 million yuan, down 10.4% [1] - Combined revenue from the above two products accounted for 10.5% of total revenue [1] - Revenue from the hair loss sector was 690 million yuan, up 23.8%, accounting for 15.8% of total revenue [1] - Revenue from Mandi was 682 million yuan, up 24.0% [1] - CDMO business achieved revenue of 101 million yuan, up 76.1% [1] - Revenue from Sanofi was 642 million yuan, up 7.6% [1] Research and Development - As of the end of 1H25, the company had a rich pipeline of 30 products under research, covering areas such as hematology, oncology, autoimmune diseases, and nephrology [2] - Notable products include: - SSGJ-706 (anti-PD-1/PD-L1 bispecific antibody) approved for two Phase II clinical trials [2] - SSGJ-705 (anti-PD-1/HER2 bispecific antibody) has received FDA approval for IND in the U.S. [2] - SSS59 (MUC17/CD3/CD28 trispecific antibody) has entered Phase I clinical trials for solid tumors [2] Collaborations and Partnerships - The company continues to engage in external collaborations: - Granted Pfizer global rights to SSGJ-707 (PD-1/VEGF bispecific antibody), receiving a $1.25 billion upfront payment and potential future milestone payments exceeding $4.8 billion [2] - Collaborated with Haihe Pharmaceuticals for oral paclitaxel, which is under preliminary review for inclusion in the 2025 National Medical Insurance Directory [2] - Partnered with Hanyu Pharmaceuticals for semaglutide injection, completing patient enrollment for Phase III clinical trials [2] - Signed a collaboration with Ying'en Bio for commercialization rights of DB-1303 (HER2 ADC) in mainland China, Hong Kong, and Macau [2] Profit Forecast and Valuation - The company raised its net profit forecasts for 2025 and 2026 by 186.5% and 138.3% to 6.249 billion yuan and 5.664 billion yuan, respectively [2] - The current stock price corresponds to 11.3x and 12.3x P/E ratios for 2025 and 2026 [2] - The target price was raised by 39.9% to 36.50 HKD, implying a 14.9% upside potential [2]

Core Viewpoint - CICC has raised the net profit estimates for 2025 and 2026 for Sangfor Pharmaceuticals (01530) by 186.5% and 138.3% to CNY 6.249 billion and CNY 5.664 billion respectively, reflecting a positive outlook on the company's BD revenue recognition [1] Group 1: Financial Performance - In 1H25, the company's revenue was CNY 4.356 billion, a slight decline of 0.8% year-on-year; however, the net profit attributable to the parent company increased by 24.6% to CNY 1.358 billion, and the adjusted net profit rose by 2.1% to CNY 1.136 billion, meeting market expectations [1] - The current stock price corresponds to a price-to-earnings ratio of 11.3x for 2025 and 12.3x for 2026, with a target price raised by 39.9% to HKD 36.50, implying a potential upside of 14.9% [1] Group 2: Product Sales Performance - The sales of the company's core commercial products faced pressure in 1H25, with revenue from Teva Australia declining by 4.2% to CNY 2.371 billion, accounting for 54.4% of total revenue; revenue from Yibiao fell by 12.1% to CNY 346 million, and revenue from Cyberol decreased by 10.4% to CNY 110 million, together representing 10.5% of total revenue [2] - Revenue from the hair loss sector grew by 23.8% to CNY 690 million, accounting for 15.8% of total revenue, with Mandai contributing CNY 682 million, a 24.0% increase [2] - The CDMO business achieved revenue of CNY 101 million in 1H25, a significant increase of 76.1% year-on-year, while Sangfor Guojian's revenue rose by 7.6% to CNY 642 million [2] Group 3: R&D Pipeline - As of the end of 1H25, the company has a rich pipeline of 30 products under research, covering areas such as hematology and oncology, autoimmune diseases, and nephrology [3] - Notable products include SSGJ-706 (anti-PD-1/PD-L1 bispecific antibody) which has received approval for two Phase II clinical trials, and SSGJ-705 (anti-PD-1/HER2 bispecific antibody) which is currently enrolling patients for Phase II trials in China [3] Group 4: External Collaborations - The company has continued its external collaborations, granting Pfizer global rights to SSGJ-707 (PD-1/VEGF bispecific antibody) for a total of USD 12.5 billion in upfront payments and potential milestone payments exceeding USD 4.8 billion, along with double-digit sales sharing [4] - The company is also collaborating with Haihe Pharmaceuticals for oral paclitaxel, which has entered the preliminary review list for the 2025 National Medical Insurance Directory adjustment [4] - Additionally, the company has partnered with Hanyu Pharmaceuticals for the completion of patient enrollment in the Phase III clinical trial of semaglutide injection for weight loss indications [4]

Group 1 - The core viewpoint of the report is that the net profit estimates for 2025 and 2026 for Sanofi Pharmaceutical have been raised significantly by 186.5% and 138.3% to 6.249 billion yuan and 5.664 billion yuan respectively, reflecting a positive outlook on the company's performance [1] - The current stock price corresponds to a price-to-earnings ratio of 11.3 times for 2025 and 12.3 times for 2026, indicating a favorable valuation [1] - The target price has been increased by 39.9% to 36.50 HKD, which implies a potential upside of 14.9% based on a price-to-earnings ratio of 13.0 times for 2025 and 14.2 times for 2026 [1] Group 2 - In the first half of 2025, the sales of the company's core commercial products faced pressure, with revenue from Teva Australia declining by 4.2% to 2.371 billion yuan, accounting for 54.4% of total revenue [2] - The revenue from the hair loss sector grew by 23.8% to 690 million yuan, representing 15.8% of total revenue, with the product Mandi contributing 682 million yuan, a 24.0% increase [2] - The CDMO business achieved a revenue of 101 million yuan, marking a significant growth of 76.1% [2] Group 3 - The company has a rich pipeline of 30 products under research, including areas such as hematology, oncology, autoimmune diseases, and nephrology [3] - Notable products in the pipeline include SSGJ-706, which has received approval for two Phase II clinical trials for gastrointestinal tumors and non-small cell lung cancer [3] - SSGJ-705 is currently enrolling patients for Phase II trials in China, with FDA approval for IND in the United States [3] Group 4 - The company continues to engage in external collaborations, having granted Pfizer global rights to SSGJ-707, receiving an upfront payment of 1.25 billion USD and potential milestone payments exceeding 4.8 billion USD [4] - The collaboration with Haihe Pharmaceuticals for oral paclitaxel has entered the preliminary review list for the 2025 National Medical Insurance Directory adjustment [4] - The partnership with Hanyu Pharmaceuticals for semaglutide injection has completed patient enrollment for Phase III clinical trials [4]

Core Viewpoint - Sanofi Pharmaceutical (01530) reported a mixed performance in its interim results for the six months ending June 30, 2025, with a slight decline in revenue but a significant increase in net profit attributable to shareholders [1] Financial Performance - The company reported revenue of RMB 4.355 billion, a year-on-year decrease of 0.77% [1] - Net profit attributable to shareholders was RMB 1.358 billion, reflecting a year-on-year increase of 24.61% [1] - Basic earnings per share were RMB 0.57 [1] Market Position - Sanofi Pharmaceutical is recognized as a leading biotechnology company in China, with extensive experience in the research, production, and marketing of biopharmaceutical products [1] - The company holds a 63.0% market share in the platelet reduction treatment market in mainland China for its product Tevaz (recombinant human thrombopoietin) as of the first half of 2025 [1] - The company has maintained a leading position in the rhEPO market in mainland China for over twenty years, with a total market share of 41.5% as of the first half of 2025 [1] - Yisaipu, the first tumor necrosis factor α inhibitor launched in mainland China, is one of the company's core products [1] - The company also dominates the minoxidil market in mainland China with its product Mandi [1] Product Development - Sanofi Pharmaceutical is expanding its treatment areas through internal research and development as well as multiple external strategic collaborations [1]

Core Viewpoint - Sanofi Pharmaceutical's stock rose over 4% in early trading, reflecting positive market sentiment following the release of its interim results for the six months ending June 30, 2025, which showed a slight revenue decline but significant profit growth [1] Financial Performance - The company's revenue for the six months was RMB 4.355 billion, a decrease of 0.77% year-on-year [1] - Shareholder profit reached RMB 1.358 billion, representing a year-on-year increase of 24.61% [1] - Basic earnings per share were reported at RMB 0.57 [1] Market Position and Products - Sanofi Pharmaceutical is recognized as a leading biotechnology company in China, with extensive experience in the research, production, and marketing of biopharmaceutical products [1] - Key commercialized products include various biopharmaceuticals such as Tebiou, recombinant human erythropoietin products (Yibiao and Saiboer), Yisaipu, and small molecule drug Mandi [1] - Tebiou is noted as the only commercialized recombinant human thrombopoietin product globally [1] Market Share - According to IQVIA, Tebiou held a 63.0% market share in the treatment of thrombocytopenia in mainland China as of the first half of 2025 [1] - The company has maintained a leading position in the rhEPO market in mainland China for over twenty years, with a total market share of 41.5% as of the first half of 2025 [1] - Yisaipu is recognized as the first tumor necrosis factor α inhibitor launched in the mainland market [1] - Mandi dominates the minoxidil market in mainland China [1] Strategic Development - The company is expanding its treatment areas through internal research and development as well as multiple external strategic collaborations [1]

Group 1 - The core viewpoint of the article highlights the financial performance of Sanofi Pharmaceutical, reporting a revenue of RMB 4.356 billion and a net profit attributable to shareholders of RMB 1.358 billion, reflecting a year-on-year increase of 24.6% [1] - The company is recognized as a leading biotechnology firm in China, with a strong focus on the research, development, production, and marketing of biopharmaceutical products [1] - Key commercialized products include various biopharmaceuticals such as Tevaz, rhEPO products, and small molecule drugs like Mandi, with Tevaz holding a 63.0% market share in the platelet reduction treatment market in mainland China as of the first half of 2025 [1] Group 2 - As of June 30, 2025, the company is actively developing 30 key products, with 27 of them being innovative drugs in mainland China, including 18 antibody drugs and 6 other biopharmaceuticals [2] - The company has 14 products in research for hematology/oncology, 10 targeting autoimmune diseases, 3 for nephrology, 2 for dermatology, and 1 for metabolic diseases [2]

Core Viewpoint - Sanofi Pharmaceutical (01530) reported a mid-term performance for the six months ending June 30, 2025, showing a revenue of RMB 4.355 billion, a slight decrease of 0.77% year-on-year, while the profit attributable to shareholders increased by 24.61% to RMB 1.358 billion, with basic earnings per share at RMB 0.57 [1] Group 1: Company Performance - The company is recognized as a leading biotechnology firm in China, with extensive experience in the research, production, and marketing of biopharmaceutical products [1] - The core commercialized products include various biopharmaceuticals such as Tevaz, recombinant human erythropoietin products Yibiao and Saiboer, Yisaipu, and Saiputin, as well as the small molecule drug Mandi [1] - Tevaz is noted as the only commercialized recombinant human thrombopoietin product globally [1] Group 2: Market Position - According to IQVIA, Tevaz held a market share of 63.0% in the treatment market for thrombocytopenia in mainland China during the first half of 2025 [1] - The company has been a market leader in the rhEPO market in mainland China for over twenty years, with a total market share of 41.5% in the first half of 2025 [1] - Yisaipu is recognized as the first tumor necrosis factor α inhibitor product launched in the mainland market [1] - Mandi also holds a dominant position in the minoxidil market in mainland China [1] Group 3: Strategic Development - The company is expanding its treatment areas through internal research and development as well as multiple external strategic collaborations [1]

香 港 交 易 及 結 算 所 有 限 公 司 及 香 港 聯 合 交 易 所 有 限 公 司 對 本 文 件 的 內 容 概 不 負 責，對 其 準 確 性 或 完 整 性 亦 不 發 表 任 何 聲 明，並 明 確 表 示，概 不 就 因 本 文 件 的 全 部 或 任 何 部 份 內 容 所 產 生 或 因 依 賴 該 等 內 容 而 引 致 的 任 何 損 失 承 擔 任 何 責 任。 （於 開 曼 群 島 註 冊 成 立 的 有 限 公 司） （股 份 代 號：01530） (1)與輝瑞就PD-1/VEGF雙特異性抗體(SSGJ-707) 訂 立 的 許 可 協 議 生 效；及 茲 提 述 本 公 司 日 期 為 二 零 二 五 年 五 月 二 十 日 的 公 告，內 容 有 關（其 中 包 括） 與輝瑞就PD-1/VEGF雙特異性抗體(SSGJ-707)訂 立 許 可 協 議。 許 可 協 議 所 訂 明 之 所 有 先 決 條 件 已 達 成，因 此，許 可 協 議 自 二 零 二 五 年 七 月 二 十 四 日 起 生 效。 構 成 許 可 協 議 項 下 先 決 條 件 之 一 的 選 擇 ...

（於 開 曼 群 島 註 冊 成 立 的 有 限 公 司） （股 份 代 號：01530） 內幕消息公告 (1)與輝瑞就PD-1/VEGF雙特異性抗體(SSGJ-707) 訂 立 許 可 協 議； 香 港 交 易 及 結 算 所 有 限 公 司 及 香 港 聯 合 交 易 所 有 限 公 司 對 本 公 告 的 內 容 概 不 負 責，對 其 準 確 性 或 完 整 性 亦 不 發 表 任 何 聲 明，並 明 確 表 示，概 不 就 因 本 公 告 的 全 部 或 任 何 部 份 內 容 所 產 生 或 因 依 賴 該 等 內 容 而 引 致 的 任 何 損 失 承 擔 任 何 責 任。 及 (2)輝瑞可能認購若干數目的本公司新股份 本公告由三生制药（「本公司」，連 同 其 附 屬 公 司，統 稱「本集團」）根據香港聯合交 易所有限公司證券上市規則（「上市規則」）第13.09(2)條及香港法例第571章證券及 期貨條例第XIVA部項下的內幕消息條文（定 義 見 上 市 規 則）作 出。 (1) 與輝瑞就PD-1/VEGF雙特異性抗體(SSGJ-707)訂立許可協議 許可協議 本公司董事會（「董事會」）欣 然 ...